- Trials with a EudraCT protocol (110)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
110 result(s) found for: Intravenous paracetamol.
Displaying page 1 of 6.
| EudraCT Number: 2010-019488-12 | Sponsor Protocol Number: Protocol No 1 | Start Date*: 2010-12-08 |
| Sponsor Name:Joint Research Office, Barts and The London NHS Trust | ||
| Full Title: A Single Centre Prospective Randomised Study to Investigate the Metabolism of Intravenous Paracetamol in Humans | ||
| Medical condition: The study is looking at the cerebrospinal fluid pharmacokinetics of intravenous paracetamol. | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: GB (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2006-002208-32 | Sponsor Protocol Number: PAR06 | Start Date*: 2006-08-14 |
| Sponsor Name:York Hospital NHS Trust | ||
| Full Title: A comparison of the analgesic efficacy of oral and intravenous paracetamol (perfalgan) in a day case setting | ||
| Medical condition: We will perform a double blind randomised comparison of oral paracetamol versus intravenous paracetamol (Perfalgan) in patients undergoing knee arthroscopy in a day surgery setting. | ||
| Disease: | ||
| Population Age: Adults | Gender: Male, Female | |
| Trial protocol: GB (Prematurely Ended) | ||
| Trial results: View results | ||
| EudraCT Number: 2006-004578-29 | Sponsor Protocol Number: P.sitsen.01 | Start Date*: 2007-06-15 |
| Sponsor Name:Leids Universitair Medisch Centrum | ||
| Full Title: The efficacy of intravenous versus rectal paracetamol: A randomized, prospective, double-blind placebo-controlled study | ||
| Medical condition: Aims of the study 1)to compare the analgesic efficacy of intravenous versus rectal paracetamol versus placebo as assessed by VAS scores and PCA morphine consumption. 2)To assess the pharmacokinet... | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: NL (Ongoing) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2010-019678-34 | Sponsor Protocol Number: not applicable | Start Date*: 2011-07-29 |
| Sponsor Name: | ||
| Full Title: Paracetamol intravenously in neonates with a gestational age of less than 32 weeks | ||
| Medical condition: Neonatal pain | ||
| Disease: | ||
| Population Age: Preterm newborn infants, Under 18 | Gender: Male, Female | |
| Trial protocol: NL (Ongoing) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2018-005006-62 | Sponsor Protocol Number: ASZ-001 | Start Date*: 2019-12-10 | |||||||||||
| Sponsor Name:Albert Schweitzer hospital | |||||||||||||
| Full Title: Pharmacokinetics of Paracetamol before and after Roux-en-Y gastric bypass | |||||||||||||
| Medical condition: Roux-en-Y gastric bypass | |||||||||||||
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| Population Age: Adults | Gender: Male, Female | ||||||||||||
| Trial protocol: NL (Ongoing) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2009-012585-30 | Sponsor Protocol Number: 1 | Start Date*: 2009-08-21 |
| Sponsor Name:NHS Grampian Research and Development | ||
| Full Title: The pharmacokinetics of single and multiple doses of intravenous paracetamol in children | ||
| Medical condition: There is no medical condition to be investigated. This is a pharmacokinetic study to be performed in children routinely treated with intravenous paracetamol for post surgical pain in line with loca... | ||
| Disease: | ||
| Population Age: Newborns, Infants and toddlers, Children, Adolescents, Under 18 | Gender: Male, Female | |
| Trial protocol: GB (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2009-011753-41 | Sponsor Protocol Number: 0902-127 | Start Date*: 2010-12-23 |
| Sponsor Name:Neonatal intensive care unit, VU medical center Amsterdam | ||
| Full Title: Pain treatment of newborns: paracetamol rectal versus intraveneous administration, an open randomised clinical trial. | ||
| Medical condition: Pain treatment of neonates and premature neonates. | ||
| Disease: | ||
| Population Age: Preterm newborn infants, Newborns, Under 18 | Gender: Male, Female | |
| Trial protocol: NL (Ongoing) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2018-000566-11 | Sponsor Protocol Number: 39-2018 | Start Date*: 2018-06-05 |
| Sponsor Name:University of Oulu | ||
| Full Title: Extremely low gestational age infants' PARAcetamol Study | ||
| Medical condition: Open ductus arteriosus of a premature infant | ||
| Disease: | ||
| Population Age: Preterm newborn infants, Under 18 | Gender: Male, Female | |
| Trial protocol: FI (Completed) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2017-002724-25 | Sponsor Protocol Number: 08-2018-07-31 | Start Date*: 2017-11-16 | |||||||||||
| Sponsor Name:Helle Holst | |||||||||||||
| Full Title: Intravenous and oral paracetamol in neonates: safety and ethanol-drug interactions – the PARASHUTE Trial | |||||||||||||
| Medical condition: Liver toxicity following prolonged administration of i.v. or oral paracetamol | |||||||||||||
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| Population Age: Preterm newborn infants, Newborns, Under 18 | Gender: Male, Female | ||||||||||||
| Trial protocol: DK (Prematurely Ended) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2006-002370-21 | Sponsor Protocol Number: 06/Q2002/25 | Start Date*: 2006-09-20 |
| Sponsor Name:North Bristol NHS Trust | ||
| Full Title: Comparison of oral and intravenous paracetamol plasma levels when given as premedication for perioperative analgesia | ||
| Medical condition: Peri-operative analgesia | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: GB (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2008-000427-26 | Sponsor Protocol Number: | Start Date*: 2009-06-25 |
| Sponsor Name:Queen Victoria Hospital NHS Foundation Trust | ||
| Full Title: A Comparison of Pre−Medication with Oral Paracetamol versus Intravenous Paracetamol Given at Time of Induction for Postoperative Analgesia Following Wisdom Tooth Extraction | ||
| Medical condition: Pain post wisdom tooth extraction | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: GB (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2015-003177-14 | Sponsor Protocol Number: IBUPAR-Trial | Start Date*: 2016-04-06 |
| Sponsor Name: | ||
| Full Title: Paracetamol versus ibuprofen in preterm infants with a hemodynamically significant patent ductus arteriosus: a randomized clinical trial. | ||
| Medical condition: Persistent ductus arteriosus haemodynamically significant | ||
| Disease: | ||
| Population Age: Preterm newborn infants, Under 18 | Gender: Male, Female | |
| Trial protocol: ES (Ongoing) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2018-000565-36 | Sponsor Protocol Number: 38/2018 | Start Date*: 2018-06-05 |
| Sponsor Name:University of Oulu | ||
| Full Title: Paracetamol and ibuprofen/indomethacin in closing persistent ductus arteriosus | ||
| Medical condition: Patent ductus arteriosus of a premature infant | ||
| Disease: | ||
| Population Age: Preterm newborn infants, Under 18 | Gender: Male, Female | |
| Trial protocol: FI (Prematurely Ended) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2005-005575-14 | Sponsor Protocol Number: R-01270-A015 | Start Date*: 2006-08-08 |
| Sponsor Name:Baxter R&D Europe S.C.R.L | ||
| Full Title: A randomized, double-blind, placebo-controlled, single-dose, parallel-group comparison of the analgesic efficacy, safety and local tolerability of intravenous paracetamol 1% solution Bioren (test),... | ||
| Medical condition: Post-surgical dental pain after removal of one or more impacted 3rd mandibular molar(s), associated with moderate to severe pain. | ||
| Disease: | ||
| Population Age: Adults | Gender: Male, Female | |
| Trial protocol: GB (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2018-002226-22 | Sponsor Protocol Number: 2.0 | Start Date*: 2019-04-30 |
| Sponsor Name:Medical University of Vienna | ||
| Full Title: The Impact of Target Temperature Management on Drug Metabolism | ||
| Medical condition: Patients after successful cardiopulmonary resuscitation who undergo target temperature management for 24h hours | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: AT (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2004-005211-28 | Sponsor Protocol Number: 20041221 | Start Date*: 2005-07-20 |
| Sponsor Name:Department of Anesthesiology, University Hospital of Erlangen | ||
| Full Title: A double-blind placebo-controlled four period crossover study of paracetamol and tramadol in the electrical hyperalgesia model of central sensitisation in healthy volunteers | ||
| Medical condition: The primary aim of the present study is to investigate the effects of intravenous paracetamol and tramadol and their combination on the experimentally-induced central sensitization in an electrical... | ||
| Disease: | ||
| Population Age: Adults | Gender: Male, Female | |
| Trial protocol: DE (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2009-014892-31 | Sponsor Protocol Number: MAIVECMOPAIN | Start Date*: 2009-11-10 |
| Sponsor Name:ErasmusMC - Sophia | ||
| Full Title: Morphine intravenous vs. Paracetamol intravenous in children on ECMO | ||
| Medical condition: Patients treated with Extra Corporal Membrane Oxygenation (ECMO) receive morphine as standardised analgesic drug. Morphine is associated with several side effects. In these patients a non-opioid dr... | ||
| Disease: | ||
| Population Age: Preterm newborn infants, Newborns, Infants and toddlers, Children, Under 18 | Gender: Male, Female | |
| Trial protocol: NL (Ongoing) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2005-001639-30 | Sponsor Protocol Number: TramaPara8405 | Start Date*: 2006-10-02 |
| Sponsor Name:Department of Anaesthesia&Intensive Care B, Vienna Medical University | ||
| Full Title: Investigation of the antihyperalgesic effect of a combination of tramadol and paracetamol on primary and secondary hyperalgesia in an UV-B induced inflammatory skin pain model in healthy volunteers. | ||
| Medical condition: This is a volunteer study in healthy volunteers. | ||
| Disease: | ||
| Population Age: Adults | Gender: Male | |
| Trial protocol: AT (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2005-003115-74 | Sponsor Protocol Number: SM4-05 | Start Date*: 2005-10-24 |
| Sponsor Name:Dept. of Anaestesiology, University hospital in Glostrup | ||
| Full Title: Effect of paracetamol versus paracetamol combined with pregabalin versus paracetamol combined with pregabalin and dexamethason on pain and opiod requirements in patient sheduled for tonsilectomie | ||
| Medical condition: Patients scheduled for toncilectomia need postoperative paintreatment. Morphine has sideeffects: Nausea, vomiting, sedation and dizziness. These sideeffects are og couse unpleasent for the patient ... | ||
| Disease: | ||
| Population Age: Adults | Gender: Male, Female | |
| Trial protocol: DK (Prematurely Ended) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2011-002213-12 | Sponsor Protocol Number: I10 005 | Start Date*: Information not available in EudraCT | ||||||||||||||||
| Sponsor Name:CHU de Limoges | ||||||||||||||||||
| Full Title: Paracetamol and setrons : drug interactions in the management of pain after tonsillectomy in children | ||||||||||||||||||
| Medical condition: Pain | ||||||||||||||||||
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| Population Age: Children, Under 18 | Gender: Male, Female | |||||||||||||||||
| Trial protocol: FR (Ongoing) | ||||||||||||||||||
| Trial results: View results | ||||||||||||||||||
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